Matti J. Haltia, MD
Affiliations: | Pathology | University of Helsinki, Helsingfors, Finland |
Area:
http://www.biomedexperts.com/Profile.bme/521043/Matti_HaltiaGoogle:
"Matti Haltia"Bio:
http://www.duodecimlehti.fi/web/guest/arkisto?p_p_id=dlehtihaku_view_article_WAR_dlehtihaku&p_p_action=1&p_p_state=maximized&p_p_mode=view&_dlehtihaku_view_article_WAR_dlehtihaku__spage
http://www.kansalliskirjasto.fi/extra/vanhat_bulletinit/bulletin09/hi5.html
http://research.med.helsinki.fi/neuro/Tienari/publications.htm
Mean distance: 106866
Cross-listing: Neuropathology Tree
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Chen Z, Yan Yau W, Jaunmuktane Z, et al. (2020) Neuronal intranuclear inclusion disease is genetically heterogeneous. Annals of Clinical and Translational Neurology |
Kiuru-Enari SMK, Haltia M. (2013) Hereditary gelsolin amyloidosis. Handbook of Clinical Neurology. 115: 659-681 |
Haltia M, Goebel HH. (2013) The neuronal ceroid-lipofuscinoses: a historical introduction. Biochimica Et Biophysica Acta. 1832: 1795-800 |
Airaksinen EM, Iivanainen M, Karli P, et al. (2009) Hereditary recurrent brachial plexus neuropathy with dysmorphic features. Acta Neurologica Scandinavica. 71: 309-316 |
Haltia M, Tarkkanen A, Somer H, et al. (2009) Neuronal intranuclear inclusion disease. Clinical ophthalmological features and ophthalmic pathology. Acta Ophthalmologica. 64: 637-643 |
Sulkava R, Haltia M, Paetau A, et al. (2009) Clinical And Neuropathological Features In Alzheimer'S Disease Acta Neurologica Scandinavica. 65: 294-295 |
Koskiniemi M, Donner M, Majuri H, et al. (2009) Progressive myoclonus epilepsy. A clinical and histopathological study. Acta Neurologica Scandinavica. 50: 307-332 |
Santavuori P, Haltia M, Rapola J. (2008) Infantile Type of So‐called Neuronal Ceroid‐lipofuscinosis Developmental Medicine & Child Neurology. 16: 644-653 |
Salonen R, Somer M, Haltia M, et al. (2008) Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome). Clinical Genetics. 39: 287-293 |
Haltia M. (2006) The neuronal ceroid-lipofuscinoses: from past to present. Biochimica Et Biophysica Acta. 1762: 850-856 |